Canonical Allele Identifier: PA2826708598
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 236513
ClinVar RCV Id: RCV000225688 RCV000367163 RCV001729470 RCV001510510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Thr455Met
CA8083441
NM_001286130.2:c.1364C>T